introduzione
- Magnetic bead nucleic acid purification technology utilizes nano or micron superparamagnetic material as the matrix, often using black or yellowish-brown ferric oxide.
- The surface of the beads is coated with functional groups such as carboxyl, hydroxyl, or silicon groups, which facilitate nucleic acid adsorption.
- Silicon-based magnetic beads are the most common, working similarly to classical glass milk or glass fiber filter membrane purification methods.
- Magpure particles are polydisperse silica magnetic beads, comprising 50% ferric oxide at the core and 50% silica on the surface.
- This product serves various purposes including plasmid extraction, gel DNA recovery, product purification, genomic DNA and Estrazione dell'RNA, as well as viral nucleic acid extraction.
Specifiche
Caratteristiche | Specifiche |
Concentration | 100 mg/ml |
Aspetto | Suspension of black particles |
Surface functional group | Si-OH, Silanol |
Dispersibility | Polydisperse Amorphous |
Particle size | 1.5-5 μm |
Condizioni di conservazione | Temperatura ambiente, valid for up to 2 anni.
It is recommended to store at 2-8°C to prevent microbial growth. |
Magnetic response speed | 15-30 secondi |
Settling velocity | >5 minuti |
High salt-mediated binding | >2M guanidina isothiocyanate, DNA recovery up to 80% |
Alcohol mediated binding | 2M guanidine hydrochloride/isopropanol (30%), and the recovery of DNA / RNA was as high as 85% |
PEG8000 mediated binding | The recovery of DNA/RNA was up to 85% |
DNase/RNase | Non rilevata |
DNA residue | <1 ppm |
Applicazione consigliata | Plasmid extraction, gel DNA recovery, estrazione del DNA genomico, and RNA extraction. |
Principio
- High salt mediated binding: Magpure particles can selectively recover DNA molecules in solutions containing 2-4M guanidine isothiocyanate, while impurities like protein polysaccharides are not adsorbed.
- Alcohol-mediated binding: Magpure particles can selectively recover DNA/RNA molecules in solutions containing guanidine salt and alcohol (>25%), with proteins and other impurities not being adsorbed.
- After treating biological samples with a digestive solution or lysis buffer, DNA/RNA is released into the reagents from cells, organelles, and protein complexes (ribosomes and nucleosomes).
- Upon adding Magpure particles and binding solution, DNA/RNA adheres to the surface of the particles, forming the DNA/RNA bead complex.
- The magnetic field then separates and collects the magnetic beads, removing impurities such as protein with the waste liquid.
- Following two or three additional cleaning steps, the DNA/RNA magnetic bead complex is resuspended in sterilized water or TE buffer.
- DNA/RNA falls off from the surface of the magnetic beads, achieving purification.
Informazioni sull'ordine
N. CAT. | nome del prodotto | Pacchetto |
C14100 | Particelle MagPure | 100 ml |
C14101 | Particelle MagPure | 400 ml |
C14102 | Particelle MagPure | 3 X 400 ml |
C14103 | Particelle MagPure | 10 X 400 ml |
Guida all'acquisto
Caratteristiche | Particelle MagPure | Particelle MagPure N | Particelle MagPure Mr | MagPure Particles F | Legare le particelle |
Cat.no. | C1410 | C1411 | C1412 | C1414 | C1413 |
Concentration | 100mg/ml | 70mg/ml | 40mg/ml | 50mg/ml | 10mg/ml |
Form | Amorphous and Porous | Amorphous and Porous | Porous | Amorphous | Nonporous |
Surface function | Si-OH, Silica Beads | Si-OH, Silica Beads | Si-OH, Silica Beads | Si-OH, Silica Beads | COOH, Carboxyl Beads |
Dispersion | Polydisperse | Polydisperse | Monodisperse | Monodisperse | Monodisperse |
Particle Size | 1.5-5μm | 0.2-2μm | 1-1.5μm | 0.2-1.5μm | 0.8-1μm |
Color | Black | Yellowish Brown | Dark Brown | Dark Brown | Yellowish Brown |
Magnetic response | 15-30S | ~60s | ~30s | 20S | 120S |
Settling Time (1ml) | >5min | >10min | >3min | >3min | >2H |
Usage (0.2ml Sample) | 20ml | 20ml | 20-30ml | 20-30ml | 20-30ml |
DNA Recover Rate (only 4M GITC) | >80% | >80% | >80% | >80% | 0 |
DNA Recover Rate (10% PEG8000/NaCl) | >85% | >85% | >85% | >85% | >90% |
Recommended Use |
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- MagPure magnetic-particle technology combines the speed and efficiency of silica-based DNA purification with the convenience of magnetic particles.
- DNA binds to the silica surface of the magnetic particles in the presence of a chaotropic salt.
- Bound DNA is efficiently washed, significantly enhancing DNA purity.
- High-quality DNA is eluted from the magnetic particles.
- The automated purification procedure removes enzymes, nucleotides, and other contaminants and inhibitors completely.
- Purified DNA is ready for direct use in downstream applications, including sequencing and microarray analysis.
Recensioni
Non ci sono ancora recensioni.